Doxepin, a tricyclic antidepressant, binds to normal, intact astroglial cells in cultures and inhibits the isoproterenol-induced increase in cylic AMP production
- 1 December 1980
- journal article
- letter
- Published by Canadian Science Publishing in Canadian Journal of Physiology and Pharmacology
- Vol. 58 (12) , 1515-1519
- https://doi.org/10.1139/y80-230
Abstract
Doxepin binds to intact [mouse] astrocytes in primary cultures. The binding is competitively displaceable by excess cold doxepin and it is pronounced (Bmax [maximum number of binding sites] = 27 nmol/mg protein), but the affinity is rather low (Kd = 30 .mu.M). The binding is inhibited by other antidepressants (amitriptyline, desipramine, tranylcypromine, iprindole) and propranolol but not by isoproterenol. Doxepin counteracts effectively the increase in the production of cAMP evoked by isoproterenol.This publication has 5 references indexed in Scilit:
- Diazepam receptors on mouse astrocytes in primary cultures: displacement by pharmacologically active concentrations of benzodiazepines or barbituratesCanadian Journal of Physiology and Pharmacology, 1980
- Binding of a labeled antidepressant to rat brain tissueBiochemical Pharmacology, 1979
- Norepinephrine stimulated cyclic AMP accumulation in rat limbic forebrain slices: Partial mediation by a subpopulation of receptors with neither α nor β characteristicsEuropean Journal of Pharmacology, 1979
- Cellular localization of [3H]-diazepam receptorsNeuropharmacology, 1978
- Influence of tricyclic antidepressants on the adenylate cyclase-phosphodiesterase system in the rat cortexNeuropharmacology, 1976